• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

饮食限制对果蝇的比较蛋白质组学分析。

Comparative proteomics analysis of dietary restriction in Drosophila.

机构信息

Institute of Animal Genetics and Breeding, Sichuan Agricultural University, Chengdu, China.

Farm Animal Genetic Resources Exploration and Innovation Key Laboratory of Sichuan Province, Sichuan Agricultural University, Chengdu, China.

出版信息

PLoS One. 2020 Oct 16;15(10):e0240596. doi: 10.1371/journal.pone.0240596. eCollection 2020.

DOI:10.1371/journal.pone.0240596
PMID:33064752
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7567386/
Abstract

To explore the underlying mechanism of dietary restriction (DR) induced lifespan extension in fruit flies at protein level, we performed proteome sequencing in Drosophila at day 7 (young) and day 42 (old) under DR and ad libitum (AL) conditions. A total of 18629 unique peptides were identified in Uniprot, corresponding to 3,662 proteins. Among them, 383 and 409 differentially expressed proteins (DEPs) were identified from comparison between DR vs AL at day 7 and 42, respectively. Bioinformatics analysis revealed that membrane-related processes, post-transcriptional processes, spliceosome and reproduction related processes, were highlighted significantly. In addition, expression of proteins involved in pathways such as spliceosomes, oxidative phosphorylation, lysosomes, ubiquitination, and riboflavin metabolism was relatively higher during DR. A relatively large number of DEPs were found to participate in longevity and age-related disease pathways. We identified 20 proteins that were consistently regulated during DR and some of which are known to be involved in ageing, such as mTORC1, antioxidant, DNA damage repair and autophagy. In the integration analysis, we found 15 genes that were stably regulated by DR at both transcriptional as well as translational levels. Our results provided a useful dataset for further investigations on the mechanism of DR and aging.

摘要

为了在蛋白质水平上探索饮食限制(DR)延长果蝇寿命的潜在机制,我们在 DR 和随意进食(AL)条件下,对第 7 天(年轻)和第 42 天(年老)的果蝇进行了蛋白质组测序。在 Uniprot 中鉴定出了 18629 个独特的肽,对应 3662 种蛋白质。其中,在第 7 天和第 42 天的 DR 与 AL 比较中,分别鉴定出 383 种和 409 种差异表达蛋白(DEPs)。生物信息学分析显示,膜相关过程、转录后过程、剪接体和生殖相关过程显著突出。此外,在 DR 期间,参与剪接体、氧化磷酸化、溶酶体、泛素化和核黄素代谢等途径的蛋白质表达相对较高。大量的 DEPs 被发现参与长寿和与年龄相关的疾病途径。我们鉴定出 20 种在 DR 期间持续调节的蛋白质,其中一些已知与衰老有关,如 mTORC1、抗氧化剂、DNA 损伤修复和自噬。在整合分析中,我们发现 15 个基因在转录和翻译水平都受到 DR 的稳定调节。我们的结果为进一步研究 DR 和衰老的机制提供了有用的数据集。

相似文献

1
Comparative proteomics analysis of dietary restriction in Drosophila.饮食限制对果蝇的比较蛋白质组学分析。
PLoS One. 2020 Oct 16;15(10):e0240596. doi: 10.1371/journal.pone.0240596. eCollection 2020.
2
Genetic and metabolomic architecture of variation in diet restriction-mediated lifespan extension in Drosophila.饮食限制介导的果蝇寿命延长的遗传和代谢组学结构。
PLoS Genet. 2020 Jul 9;16(7):e1008835. doi: 10.1371/journal.pgen.1008835. eCollection 2020 Jul.
3
Dietary switch reveals fast coordinated gene expression changes in Drosophila melanogaster.饮食转换揭示了黑腹果蝇中快速协调的基因表达变化。
Aging (Albany NY). 2014 May;6(5):355-68. doi: 10.18632/aging.100662.
4
Analysis of Drosophila melanogaster Lifespan.黑腹果蝇寿命分析。
Methods Mol Biol. 2020;2144:47-56. doi: 10.1007/978-1-0716-0592-9_4.
5
Dietary restriction in Drosophila.果蝇中的饮食限制
Mech Ageing Dev. 2005 Sep;126(9):938-50. doi: 10.1016/j.mad.2005.03.023.
6
G×G×E for lifespan in Drosophila: mitochondrial, nuclear, and dietary interactions that modify longevity.果蝇寿命的基因×基因×环境互作:影响寿命的线粒体、细胞核及饮食相互作用
PLoS Genet. 2014 May 15;10(5):e1004354. doi: 10.1371/journal.pgen.1004354. eCollection 2014.
7
Role of dFOXO in lifespan extension by dietary restriction in Drosophila melanogaster: not required, but its activity modulates the response.dFOXO在果蝇饮食限制延长寿命中的作用:非必需,但它的活性调节反应。
Aging Cell. 2008 Mar;7(2):187-98. doi: 10.1111/j.1474-9726.2007.00362.x. Epub 2008 Jan 30.
8
Drosophila lifespan control by dietary restriction independent of insulin-like signaling.通过饮食限制对果蝇寿命的控制,与胰岛素样信号传导无关。
Aging Cell. 2008 Mar;7(2):199-206. doi: 10.1111/j.1474-9726.2008.00373.x. Epub 2008 Jan 21.
9
Testing evolutionary explanations for the lifespan benefit of dietary restriction in fruit flies (Drosophila melanogaster).检测饮食限制对果蝇(Drosophila melanogaster)寿命延长的进化解释。
Evolution. 2021 Feb;75(2):450-463. doi: 10.1111/evo.14146. Epub 2021 Jan 12.
10
Nutritional regimens with periodically recurring phases of dietary restriction extend lifespan in Drosophila.周期性限制饮食的营养方案可延长果蝇的寿命。
FASEB J. 2018 Apr;32(4):1993-2003. doi: 10.1096/fj.201700934R. Epub 2018 Jan 5.

引用本文的文献

1
Genome-Wide Search for Gene Mutations Likely Conferring Insecticide Resistance in the Common Bed Bug, .全基因组搜索可能赋予臭虫抗杀虫剂能力的基因突变
Insects. 2024 Sep 24;15(10):737. doi: 10.3390/insects15100737.
2
High sugar diets can increase susceptibility to bacterial infection in Drosophila melanogaster.高糖饮食会增加果蝇对细菌感染的易感性。
PLoS Pathog. 2024 Aug 12;20(8):e1012447. doi: 10.1371/journal.ppat.1012447. eCollection 2024 Aug.
3
Metabolic Syndrome: Lessons from Rodent and Models.代谢综合征:啮齿动物模型的启示。

本文引用的文献

1
A Quantitative Proteome Map of the Human Body.人体定量蛋白质组图谱。
Cell. 2020 Oct 1;183(1):269-283.e19. doi: 10.1016/j.cell.2020.08.036. Epub 2020 Sep 10.
2
Region-Specific Proteome Changes of the Intestinal Epithelium during Aging and Dietary Restriction.衰老和饮食限制期间肠道上皮的区域特异性蛋白质组变化
Cell Rep. 2020 Apr 28;31(4):107565. doi: 10.1016/j.celrep.2020.107565.
3
Signaling Network of Forkhead Family of Transcription Factors (FOXO) in Dietary Restriction.饮食限制中的叉头框转录因子家族(FOXO)信号网络。
Biomed Res Int. 2022 Jun 22;2022:5850507. doi: 10.1155/2022/5850507. eCollection 2022.
4
Nutrition, longevity and disease: From molecular mechanisms to interventions.营养、长寿与疾病:从分子机制到干预措施。
Cell. 2022 Apr 28;185(9):1455-1470. doi: 10.1016/j.cell.2022.04.002.
Cells. 2019 Dec 31;9(1):100. doi: 10.3390/cells9010100.
4
Discovery proteomics in aging human skeletal muscle finds change in spliceosome, immunity, proteostasis and mitochondria.衰老人类骨骼肌中的发现蛋白质组学发现剪接体、免疫、蛋白质稳态和线粒体的变化。
Elife. 2019 Oct 23;8:e49874. doi: 10.7554/eLife.49874.
5
Alternative splicing in Alzheimer's disease.阿尔茨海默病中的可变剪接。
Aging Clin Exp Res. 2021 Apr;33(4):747-758. doi: 10.1007/s40520-019-01360-x. Epub 2019 Oct 3.
6
Multidimensional Proteomics Identifies Declines in Protein Homeostasis and Mitochondria as Early Signals for Normal Aging and Age-associated Disease in .多维蛋白质组学鉴定出蛋白质动态平衡和线粒体的下降是正常衰老和与年龄相关疾病的早期信号。
Mol Cell Proteomics. 2019 Oct;18(10):2078-2088. doi: 10.1074/mcp.RA119.001621. Epub 2019 Aug 21.
7
Protein Kinase D Is Dispensable for Development and Survival of .蛋白激酶 D 在 …… 的发育和存活中是可有可无的。
G3 (Bethesda). 2019 Aug 8;9(8):2477-2487. doi: 10.1534/g3.119.400307.
8
The Impact of Caloric Restriction on the Epigenetic Signatures of Aging.热量限制对衰老表观遗传特征的影响。
Int J Mol Sci. 2019 Apr 24;20(8):2022. doi: 10.3390/ijms20082022.
9
Proteome changes in the aging head.衰老头部的蛋白质组变化
Int J Mass Spectrom. 2018 Feb;425:36-46. doi: 10.1016/j.ijms.2018.01.003. Epub 2018 Jan 10.
10
Autophagy-Mediated Cholesterol Trafficking Controls Steroid Production.自噬调控胆固醇转运控制类固醇生成。
Dev Cell. 2019 Mar 11;48(5):659-671.e4. doi: 10.1016/j.devcel.2019.01.007. Epub 2019 Feb 21.